Determination of Cytochrome P450 2D6 (CYP2D6) Gene Copy Number by Real-Time Quantitative PCR

Gene dosage by real-time quantitative PCR has proved to be accurate for measuring gene copy number. The aim of this study was to apply this approach to the CYP2D6 gene to allow for rapid identification of poor and ultrarapid metabolizers (0, 1, or more than 2 gene copy number). Using the 2−ΔΔCt calc...

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Main Authors: Laurent Bodin, Philippe H. Beaune, Marie-Anne Loriot
Format: Article
Language:English
Published: Hindawi Limited 2005-01-01
Series:Journal of Biomedicine and Biotechnology
Online Access:http://dx.doi.org/10.1155/JBB.2005.248
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spelling doaj-3a672351060c4eec8d67da97f0febc7d2020-11-25T00:48:42ZengHindawi LimitedJournal of Biomedicine and Biotechnology1110-72431110-72512005-01-012005324825310.1155/JBB.2005.248Determination of Cytochrome P450 2D6 (CYP2D6) Gene Copy Number by Real-Time Quantitative PCRLaurent Bodin0Philippe H. Beaune1Marie-Anne Loriot2INSERM UMRS 490, Université René Descartes - Paris 5, 45 rue des Saints-Péres, Paris 75270, FranceINSERM UMRS 490, Université René Descartes - Paris 5, 45 rue des Saints-Péres, Paris 75270, FranceINSERM UMRS 490, Université René Descartes - Paris 5, 45 rue des Saints-Péres, Paris 75270, FranceGene dosage by real-time quantitative PCR has proved to be accurate for measuring gene copy number. The aim of this study was to apply this approach to the CYP2D6 gene to allow for rapid identification of poor and ultrarapid metabolizers (0, 1, or more than 2 gene copy number). Using the 2−ΔΔCt calculation method and a duplex reaction, the number of CYP2D6 gene copies was determined. Quantitative PCR was performed on 43 samples previously analyzed by Southern blotting and long PCR including 20 samples with a heterozygous deletion, 11 with normal copy number (2 copies), and 12 samples with duplicated genes. The average ratio ranged from 1.02 to 1.28, 1.85 to 2.21, and 2.55 to 3.30, respectively, for the samples with 1 copy, 2 copies, and 3 copies. This study shows that this method is sensitive enough to detect either a heterozygous gene deletion or duplication.http://dx.doi.org/10.1155/JBB.2005.248
collection DOAJ
language English
format Article
sources DOAJ
author Laurent Bodin
Philippe H. Beaune
Marie-Anne Loriot
spellingShingle Laurent Bodin
Philippe H. Beaune
Marie-Anne Loriot
Determination of Cytochrome P450 2D6 (CYP2D6) Gene Copy Number by Real-Time Quantitative PCR
Journal of Biomedicine and Biotechnology
author_facet Laurent Bodin
Philippe H. Beaune
Marie-Anne Loriot
author_sort Laurent Bodin
title Determination of Cytochrome P450 2D6 (CYP2D6) Gene Copy Number by Real-Time Quantitative PCR
title_short Determination of Cytochrome P450 2D6 (CYP2D6) Gene Copy Number by Real-Time Quantitative PCR
title_full Determination of Cytochrome P450 2D6 (CYP2D6) Gene Copy Number by Real-Time Quantitative PCR
title_fullStr Determination of Cytochrome P450 2D6 (CYP2D6) Gene Copy Number by Real-Time Quantitative PCR
title_full_unstemmed Determination of Cytochrome P450 2D6 (CYP2D6) Gene Copy Number by Real-Time Quantitative PCR
title_sort determination of cytochrome p450 2d6 (cyp2d6) gene copy number by real-time quantitative pcr
publisher Hindawi Limited
series Journal of Biomedicine and Biotechnology
issn 1110-7243
1110-7251
publishDate 2005-01-01
description Gene dosage by real-time quantitative PCR has proved to be accurate for measuring gene copy number. The aim of this study was to apply this approach to the CYP2D6 gene to allow for rapid identification of poor and ultrarapid metabolizers (0, 1, or more than 2 gene copy number). Using the 2−ΔΔCt calculation method and a duplex reaction, the number of CYP2D6 gene copies was determined. Quantitative PCR was performed on 43 samples previously analyzed by Southern blotting and long PCR including 20 samples with a heterozygous deletion, 11 with normal copy number (2 copies), and 12 samples with duplicated genes. The average ratio ranged from 1.02 to 1.28, 1.85 to 2.21, and 2.55 to 3.30, respectively, for the samples with 1 copy, 2 copies, and 3 copies. This study shows that this method is sensitive enough to detect either a heterozygous gene deletion or duplication.
url http://dx.doi.org/10.1155/JBB.2005.248
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